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水合肼 → (5,7-Difluoroquinolin-6-yl)methanamine

HRID 1892425
笔记
打印预览

反应方程式

HRID 1892425 反应方程式
[F:1][C:2]1[C:11]([CH2:12][N:13]2C(=O)C3C(=CC=CC=3)C2=O)=[C:10]([F:24])[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2.O.NN>CO>[F:1][C:2]1[C:11]([CH2:12][NH2:13])=[C:10]([F:24])[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2
参与物实验过程后处理来源与证据反应笔记

参与物

4

反应物 2

HCID 24654水合肼HCID 698103402-(5,7-Difluoroquinolin-6-ylmethyl)isoindoline-1,3-dione

产物 1

HCID 66994774(5,7-Difluoroquinolin-6-yl)methanamine收率 88.4%

试剂、催化剂与溶剂 1

HCID 887Methanol溶剂

实验过程

To a solution of 2-(5,7-difluoroquinolin-6-ylmethyl)isoindoline-1,3-dione (5.10 g, 15.73 mmol) in CH3OH (150 mL) was added hydrazine monohydrate (0.50 g, 15.73 mmol). The solution was heated at reflux for 3 h. After cooling, the mixture was filtered through celite. The filtrate was concentrated in vacuo. EtOAc was added to dilute the residue, filtered and concentrated in vacuo to afford (5,7-difluoroquinolin-6-yl)methanamine (2.70 g, 88%). 1H-NMR (400 MHz, CDCl3) δ ppm 8.93 (d, 1H), 8.38 (d, 1H), 7.59 (d, 1H), 7.43 (m, 1H), 4.12 (s, 2H). LCMS (method B): [MH]+=195.0, tR=0.17 min.

本页导航参与物实验过程后处理来源与证据反应笔记

后处理

  1. temperatureThe solution was heated
  2. temperatureat reflux for 3 h
  3. temperatureAfter cooling
  4. filtrationthe mixture was filtered through celite
  5. concentrationThe filtrate was concentrated in vacuo
  6. additionEtOAc was added
  7. additionto dilute the residue
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

来源与证据

ORD记录
ord-561094c7dbae406e93dfcc0b312bea16
来源数据集
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08507676B2

反应笔记

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